obsolete_Weiss-Kruszka syndrome true http://purl.obolibrary.org/obo/MONDO_0032836 An autosomal dominant, multiple congenital anomaly syndrome with variable expressivity and complete penetrance. Patients manifest developmental delay, hypotonia, feeding difficulties, craniofacial abnormalities including ptosis, abnormal head shape, downslanting palpebral fissures, metopic ridging, and craniosynostosis. Variable congenital heart defects can be observed in some patients. A few patients show agenesis of the corpus callosum on brain imaging. OMIM:618619 Replaced by Mondo term MONDO_0032836 which has the same label. Use: http://purl.obolibrary.org/obo/MONDO_0032836 paola 3.88.0